Label: MUCUS RELIEF DM- dextromethorphan hbr 20mg guaifenesin 400mg tablet
- NDC Code(s): 72090-027-01
- Packager: Pioneer Life Sciences, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 4, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each tablet)
- Purpose
-
USES:
• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
• temporarily relieves
o cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
o the intensity of coughing
o the impulse to cough to help you get to sleep - WARNINGS:
-
Do not use
- for children under 12 year of age
- if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
- OTHER INFORMATION:
- INACTIVE INGREDIENTS:
- QUESTIONS OR COMMENTS?
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM
dextromethorphan hbr 20mg guaifenesin 400mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72090-027 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 400 mg Inactive Ingredients Ingredient Name Strength microcrystalline cellulose (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) STEARIC ACID (UNII: 4ELV7Z65AP) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM STEARATE (UNII: 70097M6I30) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) Product Characteristics Color white Score no score Shape OVAL Size 16mm Flavor Imprint Code ET16 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72090-027-01 150 in 1 BOTTLE; Type 0: Not a Combination Product 10/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 10/04/2024 Labeler - Pioneer Life Sciences, LLC (014092742)